Diabetes predicts severity of COVID‐19 infection in a retrospective cohort: A mediatory role of the inflammatory biomarker C‐reactive protein
Diabetes is a risk factor for developing severe COVID‐19, but the pathogenesis remains unclear. We investigated if the association of diabetes and COVID‐19 severity may be mediated by inflammation. We also hypothesized that this increased risk may extend to prediabetes. Hospitalized patients in Sing...
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Published in | Journal of medical virology Vol. 93; no. 5; pp. 3023 - 3032 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Wiley Subscription Services, Inc
01.05.2021
John Wiley and Sons Inc |
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Abstract | Diabetes is a risk factor for developing severe COVID‐19, but the pathogenesis remains unclear. We investigated if the association of diabetes and COVID‐19 severity may be mediated by inflammation. We also hypothesized that this increased risk may extend to prediabetes. Hospitalized patients in Singapore with COVID‐19 were subdivided into three groups in a retrospective cohort: normoglycemia (HbA1c: ≤5.6%), prediabetes (HbA1c: 5.7%–6.4%) and diabetes (HbA1c: ≥6.5%). The primary outcome of severe COVID‐19 was defined by respiratory rate ≥30, SpO2 ≤93% or intensive care unit admission. The association between clinical factors on severe COVID‐19 outcome was analyzed by cox regression. Adjusted mediation analysis of C‐reactive protein (CRP) on the relationship between diabetes and severe COVID‐19 was performed. Of 1042 hospitalized patients, mean age 39 ± 11 years, 13% had diabetes, 9% prediabetes and 78% normoglycemia. Severe COVID‐19 occurred in 4.9% of subjects. Compared to normoglycemia, diabetes was significantly associated with severe COVID‐19 on both univariate (hazard ratio [HR]: 9.94; 95% confidence interval [CI]: 5.54–17.84; p < .001) and multivariate analysis (HR: 3.99; 95% CI: 1.92–8.31; p < .001), while prediabetes was not a risk factor (HR: 0.94; 95% CI: 0.22–4.03; p = .929). CRP, a biomarker of inflammation, mediated 32.7% of the total association between diabetes and severe COVID‐19 outcome. In conclusion, CRP is a partial mediator of the association between diabetes and severe COVID‐19 infection, confirming that inflammation is important in the pathogenesis of severe COVID‐19 in diabetes.
Research Highlights
Inflammation, as measured by the biomarker C‐reactive protein, partially mediates the association between diabetes and adverse COVID‐19 outcomes, including the risk of developing severe COVID‐19, dyspnea, need for intensive care unit and length of stay.
Level of glycaemia in patients with diabetes does not correlate with severe COVID‐19.
Prediabetes is not an adverse prognostic marker in COVID‐19. |
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AbstractList | Diabetes is a risk factor for developing severe COVID-19, but the pathogenesis remains unclear. We investigated if the association of diabetes and COVID-19 severity may be mediated by inflammation. We also hypothesized that this increased risk may extend to prediabetes. Hospitalized patients in Singapore with COVID-19 were subdivided into three groups in a retrospective cohort: normoglycemia (HbA1c: ≤5.6%), prediabetes (HbA1c: 5.7%-6.4%) and diabetes (HbA1c: ≥6.5%). The primary outcome of severe COVID-19 was defined by respiratory rate ≥30, SpO2 ≤93% or intensive care unit admission. The association between clinical factors on severe COVID-19 outcome was analyzed by cox regression. Adjusted mediation analysis of C-reactive protein (CRP) on the relationship between diabetes and severe COVID-19 was performed. Of 1042 hospitalized patients, mean age 39 ± 11 years, 13% had diabetes, 9% prediabetes and 78% normoglycemia. Severe COVID-19 occurred in 4.9% of subjects. Compared to normoglycemia, diabetes was significantly associated with severe COVID-19 on both univariate (hazard ratio [HR]: 9.94; 95% confidence interval [CI]: 5.54-17.84; p < .001) and multivariate analysis (HR: 3.99; 95% CI: 1.92-8.31; p < .001), while prediabetes was not a risk factor (HR: 0.94; 95% CI: 0.22-4.03; p = .929). CRP, a biomarker of inflammation, mediated 32.7% of the total association between diabetes and severe COVID-19 outcome. In conclusion, CRP is a partial mediator of the association between diabetes and severe COVID-19 infection, confirming that inflammation is important in the pathogenesis of severe COVID-19 in diabetes. Inflammation, as measured by the biomarker C‐reactive protein, partially mediates the association between diabetes and adverse COVID‐19 outcomes, including the risk of developing severe COVID‐19, dyspnea, need for intensive care unit and length of stay. Level of glycaemia in patients with diabetes does not correlate with severe COVID‐19. Prediabetes is not an adverse prognostic marker in COVID‐19. Diabetes is a risk factor for developing severe COVID-19, but the pathogenesis remains unclear. We investigated if the association of diabetes and COVID-19 severity may be mediated by inflammation. We also hypothesized that this increased risk may extend to prediabetes. Hospitalized patients in Singapore with COVID-19 were subdivided into three groups in a retrospective cohort: normoglycemia (HbA1c: ≤5.6%), prediabetes (HbA1c: 5.7%-6.4%) and diabetes (HbA1c: ≥6.5%). The primary outcome of severe COVID-19 was defined by respiratory rate ≥30, SpO2 ≤93% or intensive care unit admission. The association between clinical factors on severe COVID-19 outcome was analyzed by cox regression. Adjusted mediation analysis of C-reactive protein (CRP) on the relationship between diabetes and severe COVID-19 was performed. Of 1042 hospitalized patients, mean age 39 ± 11 years, 13% had diabetes, 9% prediabetes and 78% normoglycemia. Severe COVID-19 occurred in 4.9% of subjects. Compared to normoglycemia, diabetes was significantly associated with severe COVID-19 on both univariate (hazard ratio [HR]: 9.94; 95% confidence interval [CI]: 5.54-17.84; p < .001) and multivariate analysis (HR: 3.99; 95% CI: 1.92-8.31; p < .001), while prediabetes was not a risk factor (HR: 0.94; 95% CI: 0.22-4.03; p = .929). CRP, a biomarker of inflammation, mediated 32.7% of the total association between diabetes and severe COVID-19 outcome. In conclusion, CRP is a partial mediator of the association between diabetes and severe COVID-19 infection, confirming that inflammation is important in the pathogenesis of severe COVID-19 in diabetes.Diabetes is a risk factor for developing severe COVID-19, but the pathogenesis remains unclear. We investigated if the association of diabetes and COVID-19 severity may be mediated by inflammation. We also hypothesized that this increased risk may extend to prediabetes. Hospitalized patients in Singapore with COVID-19 were subdivided into three groups in a retrospective cohort: normoglycemia (HbA1c: ≤5.6%), prediabetes (HbA1c: 5.7%-6.4%) and diabetes (HbA1c: ≥6.5%). The primary outcome of severe COVID-19 was defined by respiratory rate ≥30, SpO2 ≤93% or intensive care unit admission. The association between clinical factors on severe COVID-19 outcome was analyzed by cox regression. Adjusted mediation analysis of C-reactive protein (CRP) on the relationship between diabetes and severe COVID-19 was performed. Of 1042 hospitalized patients, mean age 39 ± 11 years, 13% had diabetes, 9% prediabetes and 78% normoglycemia. Severe COVID-19 occurred in 4.9% of subjects. Compared to normoglycemia, diabetes was significantly associated with severe COVID-19 on both univariate (hazard ratio [HR]: 9.94; 95% confidence interval [CI]: 5.54-17.84; p < .001) and multivariate analysis (HR: 3.99; 95% CI: 1.92-8.31; p < .001), while prediabetes was not a risk factor (HR: 0.94; 95% CI: 0.22-4.03; p = .929). CRP, a biomarker of inflammation, mediated 32.7% of the total association between diabetes and severe COVID-19 outcome. In conclusion, CRP is a partial mediator of the association between diabetes and severe COVID-19 infection, confirming that inflammation is important in the pathogenesis of severe COVID-19 in diabetes. Diabetes is a risk factor for developing severe COVID‐19, but the pathogenesis remains unclear. We investigated if the association of diabetes and COVID‐19 severity may be mediated by inflammation. We also hypothesized that this increased risk may extend to prediabetes. Hospitalized patients in Singapore with COVID‐19 were subdivided into three groups in a retrospective cohort: normoglycemia (HbA1c: ≤5.6%), prediabetes (HbA1c: 5.7%–6.4%) and diabetes (HbA1c: ≥6.5%). The primary outcome of severe COVID‐19 was defined by respiratory rate ≥30, SpO2 ≤93% or intensive care unit admission. The association between clinical factors on severe COVID‐19 outcome was analyzed by cox regression. Adjusted mediation analysis of C‐reactive protein (CRP) on the relationship between diabetes and severe COVID‐19 was performed. Of 1042 hospitalized patients, mean age 39 ± 11 years, 13% had diabetes, 9% prediabetes and 78% normoglycemia. Severe COVID‐19 occurred in 4.9% of subjects. Compared to normoglycemia, diabetes was significantly associated with severe COVID‐19 on both univariate (hazard ratio [HR]: 9.94; 95% confidence interval [CI]: 5.54–17.84; p < .001) and multivariate analysis (HR: 3.99; 95% CI: 1.92–8.31; p < .001), while prediabetes was not a risk factor (HR: 0.94; 95% CI: 0.22–4.03; p = .929). CRP, a biomarker of inflammation, mediated 32.7% of the total association between diabetes and severe COVID‐19 outcome. In conclusion, CRP is a partial mediator of the association between diabetes and severe COVID‐19 infection, confirming that inflammation is important in the pathogenesis of severe COVID‐19 in diabetes. Research Highlights Inflammation, as measured by the biomarker C‐reactive protein, partially mediates the association between diabetes and adverse COVID‐19 outcomes, including the risk of developing severe COVID‐19, dyspnea, need for intensive care unit and length of stay. Level of glycaemia in patients with diabetes does not correlate with severe COVID‐19. Prediabetes is not an adverse prognostic marker in COVID‐19. Diabetes is a risk factor for developing severe COVID‐19, but the pathogenesis remains unclear. We investigated if the association of diabetes and COVID‐19 severity may be mediated by inflammation. We also hypothesized that this increased risk may extend to prediabetes. Hospitalized patients in Singapore with COVID‐19 were subdivided into three groups in a retrospective cohort: normoglycemia (HbA1c: ≤5.6%), prediabetes (HbA1c: 5.7%–6.4%) and diabetes (HbA1c: ≥6.5%). The primary outcome of severe COVID‐19 was defined by respiratory rate ≥30, SpO2 ≤93% or intensive care unit admission. The association between clinical factors on severe COVID‐19 outcome was analyzed by cox regression. Adjusted mediation analysis of C‐reactive protein (CRP) on the relationship between diabetes and severe COVID‐19 was performed. Of 1042 hospitalized patients, mean age 39 ± 11 years, 13% had diabetes, 9% prediabetes and 78% normoglycemia. Severe COVID‐19 occurred in 4.9% of subjects. Compared to normoglycemia, diabetes was significantly associated with severe COVID‐19 on both univariate (hazard ratio [HR]: 9.94; 95% confidence interval [CI]: 5.54–17.84; p < .001) and multivariate analysis (HR: 3.99; 95% CI: 1.92–8.31; p < .001), while prediabetes was not a risk factor (HR: 0.94; 95% CI: 0.22–4.03; p = .929). CRP, a biomarker of inflammation, mediated 32.7% of the total association between diabetes and severe COVID‐19 outcome. In conclusion, CRP is a partial mediator of the association between diabetes and severe COVID‐19 infection, confirming that inflammation is important in the pathogenesis of severe COVID‐19 in diabetes. Inflammation, as measured by the biomarker C‐reactive protein, partially mediates the association between diabetes and adverse COVID‐19 outcomes, including the risk of developing severe COVID‐19, dyspnea, need for intensive care unit and length of stay. Level of glycaemia in patients with diabetes does not correlate with severe COVID‐19. Prediabetes is not an adverse prognostic marker in COVID‐19. |
Author | Koh, Huilin Ooi, Say Tat Moh, Angela Mei Chung Low, Serena Kiat Mun Hoong, Caroline Wei Shan Tan, Seng Kiong Lin, Jaime Hui Xian Yeoh, Ester Lin, Yi |
AuthorAffiliation | 2 Clinical Research Unit Khoo Teck Puat Hospital Singapore Singapore Singapore 5 Clinical Epidemiology Unit Khoo Teck Puat Hospital Singapore Singapore Singapore 1 Division of Endocrinology, Department of Medicine Woodlands Health Campus Singapore Singapore Singapore 3 Diabetes Centre, Admiralty Medical Centre Khoo Teck Puat Hospital Singapore Singapore Singapore 6 Division of Infectious Disease, Department of General Medicine Khoo Teck Puat Hospital Singapore Singapore Singapore 4 Division of Endocrinology, Department of General Medicine Khoo Teck Puat Hospital Singapore Singapore Singapore |
AuthorAffiliation_xml | – name: 1 Division of Endocrinology, Department of Medicine Woodlands Health Campus Singapore Singapore Singapore – name: 5 Clinical Epidemiology Unit Khoo Teck Puat Hospital Singapore Singapore Singapore – name: 6 Division of Infectious Disease, Department of General Medicine Khoo Teck Puat Hospital Singapore Singapore Singapore – name: 3 Diabetes Centre, Admiralty Medical Centre Khoo Teck Puat Hospital Singapore Singapore Singapore – name: 2 Clinical Research Unit Khoo Teck Puat Hospital Singapore Singapore Singapore – name: 4 Division of Endocrinology, Department of General Medicine Khoo Teck Puat Hospital Singapore Singapore Singapore |
Author_xml | – sequence: 1 givenname: Huilin surname: Koh fullname: Koh, Huilin organization: Woodlands Health Campus Singapore – sequence: 2 givenname: Angela Mei Chung surname: Moh fullname: Moh, Angela Mei Chung organization: Khoo Teck Puat Hospital Singapore – sequence: 3 givenname: Ester orcidid: 0000-0002-2686-9412 surname: Yeoh fullname: Yeoh, Ester organization: Khoo Teck Puat Hospital Singapore – sequence: 4 givenname: Yi surname: Lin fullname: Lin, Yi organization: Khoo Teck Puat Hospital Singapore – sequence: 5 givenname: Serena Kiat Mun surname: Low fullname: Low, Serena Kiat Mun organization: Khoo Teck Puat Hospital Singapore – sequence: 6 givenname: Say Tat surname: Ooi fullname: Ooi, Say Tat organization: Khoo Teck Puat Hospital Singapore – sequence: 7 givenname: Seng Kiong orcidid: 0000-0002-4754-2152 surname: Tan fullname: Tan, Seng Kiong organization: Khoo Teck Puat Hospital Singapore – sequence: 8 givenname: Jaime Hui Xian surname: Lin fullname: Lin, Jaime Hui Xian organization: Woodlands Health Campus Singapore – sequence: 9 givenname: Caroline Wei Shan orcidid: 0000-0002-5206-5477 surname: Hoong fullname: Hoong, Caroline Wei Shan email: caroline_hoong@whc.sg organization: Woodlands Health Campus Singapore |
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Snippet | Diabetes is a risk factor for developing severe COVID‐19, but the pathogenesis remains unclear. We investigated if the association of diabetes and COVID‐19... Inflammation, as measured by the biomarker C‐reactive protein, partially mediates the association between diabetes and adverse COVID‐19 outcomes, including the... Diabetes is a risk factor for developing severe COVID-19, but the pathogenesis remains unclear. We investigated if the association of diabetes and COVID-19... |
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SubjectTerms | Adult Biomarkers Biomarkers - blood Blood glucose C-reactive protein C-Reactive Protein - metabolism Confidence intervals COVID-19 COVID-19 - blood COVID-19 - diagnosis COVID-19 - epidemiology Diabetes Diabetes mellitus Diabetes Mellitus - blood Diabetes Mellitus - epidemiology Dyspnea Female Health risks Hospitalization - statistics & numerical data Humans Infections Inflammation Intensive care Male mediation Middle Aged Multivariate analysis Pathogenesis prediabetes Prognosis Proportional Hazards Models Proteins Regression analysis Respiration Respiratory rate Retrospective Studies Risk analysis Risk Factors SARS-CoV-2 severe COVID‐19 Severity of Illness Index Singapore - epidemiology Statistical analysis Virology |
Title | Diabetes predicts severity of COVID‐19 infection in a retrospective cohort: A mediatory role of the inflammatory biomarker C‐reactive protein |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmv.26837 https://www.ncbi.nlm.nih.gov/pubmed/33527464 https://www.proquest.com/docview/2509226126 https://www.proquest.com/docview/2485515786 https://pubmed.ncbi.nlm.nih.gov/PMC8013709 |
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